Ability to walk at least 10m with maximum 1 person assist
Physician approval for patient participation
Able to safely fit into device specifications and tolerate minimum assistance
You may not be if
≤90 days post major orthopedic surgery (i.e. hip, knee, and/or ankle joint replacement)
≤ 6 months post coronary artery bypass graft (CABG) or cardiac valve procedure
Severe osteoporosis as indicated by physician medical clearance
Serious cardiac conditions (hospitalization for myocardial infarction or heart surgery within 3 months, history of congestive heart failure, documented serious and unstable cardiac arrhythmias, hypertrophic cardiomyopathy, severe aortic stenosis, angina or dyspnea at rest or during activities of daily living)
Pregnancy
Uncontrolled hypertension
Lower extremity fracture
Modified Ashworth Spasticity ≥3 in hip flexor or extensor
Preexisting neurological disorders such as Parkinson's disease, Amyotrophic Lateral Sclerosis (ALS), Multiple Sclerosis (MS), dementia
History of: major head trauma, lower extremity amputation, non-healing ulcers of a lower extremity, ongoing active infections, legal blindness, or a history of significant psychiatric illness
Participating in any other structured outpatient, home health physical therapy program, or another clinical trial that according to the Principal Investigator is likely to affect study outcome or confound results.
Pacemakers, metal implants in the head region
History of unexplained, recurring headaches, epilepsy/seizures/skull fractures or skull deficits
Medications that lower seizure threshold
History of concussion in last 6 months
Clareo Health | Safety and Efficacy of Samsung GEMS-H Device Training in Sub-Acute and Chronic Stroke